Military Health and Nutrition Examination Study
MHANES
Stand Ready: Military Health and Nutrition Examination Study
1 other identifier
observational
650
1 country
3
Brief Summary
The Military Health and Nutrition Examination Study (MHANES) is a Department of Defense funded study conducted by Pennington Biomedical Research Center and the US Army Research Institute of Environmental Medicine. This cross-sectional study will assess, in a large, diverse sample of Army Service Members (n=600), food and supplement intake, cardiovascular health, body composition, biomarkers of nutritional status, measures of health status, injury prevalence, mental wellbeing, gut microbiome composition, and physical performance outcomes. The proposed study is modeled after the National Health and Nutrition Examination Survey (NHANES) and customized for the Army population.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2024
Typical duration for all trials
3 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 30, 2024
CompletedFirst Posted
Study publicly available on registry
April 23, 2024
CompletedStudy Start
First participant enrolled
August 24, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2026
November 12, 2025
November 1, 2025
2.3 years
March 30, 2024
November 10, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Dietary intake
24-hour dietary recalls will be collected using ASA24® to measure intake of macronutrients (protein, carbohydrate, and fat) and micronutrients (vitamins and minerals).
This study will collect one ASA24® recall at visit 1 and a second follow-up 24-hour recall 3-10 days later
Dietary quality
24-hour dietary recalls will be collected using ASA24®. Diet quality will be assessed by the healthy eating index (HEI).
This study will collect one ASA24® recall at visit 1 and a second follow-up 24-hour recall 3-10 days later
Secondary Outcomes (27)
Depression
Questionnaires will be administered one time at visit 1 (within 1-2 weeks of study enrollment).
Anxiety
Questionnaires will be administered one time at visit 1 (within 1-2 weeks of study enrollment).
Resilience
Questionnaires will be administered one time at visit 1 (within 1-2 weeks of study enrollment).
Posttraumatic stress disorder
Questionnaires will be administered one time at visit 1 (within 1-2 weeks of study enrollment).
Self-efficacy
Questionnaires will be administered one time at visit 1 (within 1-2 weeks of study enrollment).
- +22 more secondary outcomes
Study Arms (1)
Active-duty Army Service Members
All measures will be collected one time during the study, except for the dietary recall (measured two times) and urine sample for total daily energy expenditure using doubly labeled water method (measured 3 time).
Eligibility Criteria
Active-duty U.S. Army Soldiers (n=600 completers)
You may qualify if:
- U.S. Army Soldiers ≥ 18 years old
- Willing to have biological samples stored for future use
- Willing to have data linked to the Soldier Performance, Health, and Readiness (SPHERE) database
You may not qualify if:
- Soldiers under the age of 18 years
- Soldiers with an inability to understand verbal or written instructions or testing materials in English
- Soldiers relocating or getting out of the Army in the next 30 days
- Pregnant females
- Soldiers currently in Basic Training (BCT) and/or One-Station Unit Training (OSUT)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (3)
Fort Campbell
Fort Campbell, Kentucky, 42223, United States
Pennington Biomedical Research Center
Baton Rouge, Louisiana, 70808, United States
Fort Johnson
Leesville, Louisiana, 71459, United States
Related Publications (29)
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BACKGROUND
Biospecimen
Whole blood, plasma, serum, urine, and stool samples
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Claire E Berryman, PhD, RD
Pennington Biomedical Research Center
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
March 30, 2024
First Posted
April 23, 2024
Study Start
August 24, 2024
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
December 1, 2026
Last Updated
November 12, 2025
Record last verified: 2025-11
Data Sharing
- IPD Sharing
- Will not share